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| Product | Description | |
|---|---|---|
| Sodium amide | 25g Pack Size. Group: Building Blocks, Inorganic Chemicals. Formula: NaNH2. CAS No. 7782-92-5. Prepack ID 90027494-25g. Molecular Weight 39.01. See USA prepack pricing. |  |
| Sodium amide | Sodium amide. Group: Biochemicals. Grades: Highly Purified. CAS No. 7782-92-5. Pack Sizes: 250g, 500g, 1kg. US Biological Life Sciences. |  Worldwide |
| Sodium amide 98+% | Sodium amide 98+%. Group: Biochemicals. Grades: Reagent Grade. CAS No. 7782-92-5. Pack Sizes: 25g, 100g, 250g, 1Kg. US Biological Life Sciences. | Worldwide |
| 5β-Cholanic acid-3α,12α-diol N-(2-sulphoethyl)-amide sodium salt | 5β-Cholanic acid-3α,12α-diol N-(2-sulphoethyl)-amide sodium salt. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Taurodeoxycholic acid sodium salt; Taurodeoxycholate sodium salt; Sodium taurodeoxycholate hydrate. Product Category: Steroidal Compounds. Appearance: white crystalline powder. CAS No. 1180-95-6. Molecular formula: C26H44NNaO6S. Mole weight: 521.69. Purity: 0.95. IUPACName: sodium;2-[[(4R)-4-[(3R,5R,8R,9S,10S,12S,13R,14S,17R)-3,12-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoyl]amino]ethanesulfonate. Canonical SMILES: CC(CCC(=O)NCCS(=O)(=O)[O-])C1CCC2C1(C(CC3C2CCC4C3(CCC(C4)O)C)O)C.[Na+]. ECNumber: 214-652-0. Product ID: ACM1180956. Alfa Chemistry ISO 9001:2015 Certified. |  |
| 5β-Cholanic acid-3α,6α-diol N-(2-sulphoethyl)-amide sodium salt | 5β-Cholanic acid-3α,6α-diol N-(2-sulphoethyl)-amide sodium salt. Uses: Designed for use in research and industrial production. Additional or Alternative Names: taurohyodeoxycholic acid sodium hydrate; SODIUM TAUROHYODEOXYCHOLATE; Sodium taurohyodeoxycholate hydrate. Product Category: Steroidal Compounds. CAS No. 110026-03-4. Molecular formula: C26H44NNaO6S. Mole weight: 521.69. Purity: 0.95. IUPACName: TAUROHYODEOXYCHOLIC ACID SODIUM SALT. Product ID: ACM110026034. Alfa Chemistry ISO 9001:2015 Certified. | |
| 5β-CHOLANIC ACID-3α, 7α, 12α-TRIOL N-(CARBOXYMETHYL)-AMIDE SODIUM SALT | 5β-CHOLANIC ACID-3α, 7α, 12α-TRIOL N-(CARBOXYMETHYL)-AMIDE SODIUM SALT. Group: Biochemicals. Alternative Names: GLYCOCHOLIC ACID SODIUM SALTSODIUM GLYCOCHOLATE. CAS No. 863-57-0. US Biological Life Sciences. | Worldwide |
| 5β-Cholanic acid-3α-ol N-(2-sulphoethyl)-amide sodium salt | 5β-Cholanic acid-3α-ol N-(2-sulphoethyl)-amide sodium salt. Uses: Designed for use in research and industrial production. Additional or Alternative Names: SODIUM TAUROLITHOCHOLATE;SODIUM TAUROLITHOCHOLATE SODIUM SALT;TAUROLITHIOCHOLIC ACID SODIUM;TAUROLITHOCHOLIC ACID SODIUM SALT;5BETA-CHOLAN-24-OIC ACID N-[2-SULFOETHYL]AMIDE-3ALPHA-OL SODIUM SALT;5-BETA-CHOLANIC ACID-3-ALPHA-OL N-(2-SULPHOETHYL)-AMIDE SOD. Product Category: Steroidal Compounds. CAS No. 6042-32-6. Molecular formula: C26H44NNaO5S. Mole weight: 505.69. Purity: 0.95. IUPACName: sodium;2-[[(4R)-4-[(3R,5R,8R,9S,10S,13R,14S,17R)-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoyl]amino]ethanesulfonate. Canonical SMILES: CC(CCC(=O)NCCS(=O)(=O)[O-])C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C.[Na+]. Product ID: ACM6042326. Alfa Chemistry ISO 9001:2015 Certified. | |
| 5β-CHOLANIC ACID N-(CARBOXYMETHYL)-AMIDE SODIUM SALT | 5β-CHOLANIC ACID N-(CARBOXYMETHYL)-AMIDE SODIUM SALT. Group: Biochemicals. Alternative Names: GLYCOURSOCHOLANIC ACID SODIUM SALT. US Biological Life Sciences. | Worldwide |
| Mosapride Citric Amide Disodium Salt | Mosapride Citric Amide Disodium Salt is a derivative of Mosapride, which is a 5-HT4 receptor agonist and 5-HT3 receptor antagonist. It is used as a gastroprokinetic agent. Synonyms: Mosapride impurity 10; sodium 3- ( (2-chloro-5-ethoxy-4- ( ( (4- (4-fluorobenzyl) morpholin-2-yl) methyl) carbamoyl) phenyl) carbamoyl) -3-hydroxypentanedioate; 3- [ [ [2-Chloro-5-ethoxy-4- [ [ [ [4- [ (4-fluorophenyl) methyl] -2-morpholinyl] methyl] amino] carbonyl] phenyl] amino] carbonyl] -3-hydroxypentanedioic Acid Disodium Salt. Grades: 94%. Molecular formula: C27H29ClFN3Na2O9. Mole weight: 639.96. |  |
| Sodium bis (trimethylsilyl)amide | Sodium bis (trimethylsilyl)amide. Group: Biochemicals. Grades: Highly Purified. CAS No. 1070-89-9. Pack Sizes: 100g, 250g, 500g, 1kg, 2kg. Molecular Formula: C6H18NNaSi2. US Biological Life Sciences. | Worldwide |
| Sodium bis (trimethylsilyl)amide solution, 1.0 M in THF) | Sodium bis (trimethylsilyl)amide solution, 1.0 M in THF). Group: Biochemicals. Grades: Reagent Grade. CAS No. 1070-89-9. Pack Sizes: 100g, 1Kg, 500g. US Biological Life Sciences. | Worldwide |
| 1- methyl cyclopropanecarboxylic Acid Ethyl Ester | 1- methyl cyclopropanecarboxylic Acid Ethyl Ester is used to prepare secondary and tertiary amides directly with sodium diethyl diamidoaluminate as the catalyst. It is also used to study trimethylaluminium mediated amide bond formation in a continuous flow microreactor. Group: Biochemicals. Grades: Highly Purified. CAS No. 71441-76-4. Pack Sizes: 1g, 10g. Molecular Formula: C7H12O2, Molecular Weight: 128.169999999999. US Biological Life Sciences. | Worldwide |
| 2,2,6-Trimethyl-4H-1,3-dioxin-4-one | 2,2,6-Trimethyl-4H-1,3-dioxin-4-one is used in the synthesis of dihydropyrimininones as picomolar sodium iodide symporter inhibitors. Also used in the synthesis of resorcinol amide Hsp90 Inhibitor AT13387. Group: Biochemicals. Alternative Names: Diketene Acetone Adduct. Grades: Highly Purified. CAS No. 5394-63-8. Pack Sizes: 10g, 100g. Molecular Formula: C7H10O3, Molecular Weight: 142.15. US Biological Life Sciences. | Worldwide |
| 5β-Cholanic acid-3α,12α-diol N-(carboxymethyl)-amide | 5β-Cholanic acid-3α,12α-diol N-(carboxymethyl)-amide. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2-[[(4R)-4-[(3R,5R,8R,9S,10S,12S,13R,14S,17R)-3,12-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoyl]amino]acetic acid,sodium; Glycodesoxycholic acid; N-(3α,12α-Dihydroxy-24-oxocholan-24-yl)glycine; Sodium glycodeoxycholate; 3α,12α-Dihydroxy-5β-cholan-24-oic acid N-(carboxymethyl)amide. Product Category: Steroidal Compounds. CAS No. 16409-34-0. Molecular formula: C26H42NNaO5. Mole weight: 471.61. Purity: 0.97. IUPACName: Glycodeoxycholic acid sodium salt. Product ID: ACM16409340. Alfa Chemistry ISO 9001:2015 Certified. | |
| Amiloride HCl | Amiloride HCl is a relatively selective inhibitor of the epithelial sodium channel, used in the management of hypertension and congestive heart failure. Uses: Acid sensing ion channel blockers. Synonyms: Amiloride HCl anhydrous; Amiloride (hydrochloride); Amiloride hydrochloride anhydrous; MK-870 hydrochloride; N-Amidino-3,5-diamino-6-chloropyrazinecarboxamide hydrochloride. Grades: ≥ 98%. (HPLC). CAS No. 2016-88-8. Molecular formula: C6H9Cl2N7O. Mole weight: 266.09. | |
| Amiloride Hydrochloride | Sodium channel blocker. Diuretic. Group: Biochemicals. Alternative Names: 3,5-Diamino-N-(aminoiminomethyl)-6-chloro-2-pyrazinecarboxamide Hydrochloride; N-Amidino-3, 5-diamino-6-chloro cyrazinecarboxamide Monohydrochloride; N-Amidino-3,5-diamino-6-chloropyrazinamide Hydrochloride; Amipramidine; Amipramizide; Amiprazide; Colectril; Midamor; Nilurid. Grades: Highly Purified. CAS No. 2016-88-8. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Articaine hydrochloride | Articaine hydrochloride (Hoe-045) is an amide agent that can suppress or relieve pain, containing an ester group, reversibly binding to the α-subunit of the voltage-gated sodium channels within the inner cavity of the nerve, can provide effective pain relief. Articaine hydrochloride ameliorates LPS-induced acute kidney injury via inhibition of NF-κB activation and the NLRP3 inflammasome pathway [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Hoe-045. CAS No. 23964-57-0. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-B0516. |  |
| Atorvastatin Impurity F | Atorvastatin Impurity F is an impurity of Atorvastatin, a medication commonly prescribed to lower cholesterol and reduce the risk of heart attacks or strokes. Synonyms: (Amide Impurity) Sodium Salt. Grades: > 95%. CAS No. 1371615-56-3. Molecular formula: C40H47FN3O8Na. Mole weight: 739.82. | |
| AVE-0118 | AVE 0118 is a potassium channel blocker that has the potential for the treatment of sleep apnea syndrome. AVE 0118 functions without apparent effect on ventricular repolarization. Noteworthy, the atrial selective and dose-dependent prolongation of atrial refractoriness (ERP) by AVE 0118 has been claimed to be an inhibitory effect of sodium channel activity in an atrial-selective manner, and may therefore contribute to the anti-AF property of AVE0118. Synonyms: [1,1'-Biphenyl]-2-carboxamide, 2'-[[[2-(4-methoxyphenyl)acetyl]amino]methyl]-N-[2-(3-pyridinyl)ethyl]-; 2'-[[[2-(4-Methoxyphenyl)acetyl]amino]methyl]-N-[2-(3-pyridinyl)ethyl][1,1'-biphenyl]-2-carboxamide; [1,1'-Biphenyl]-2-carboxamide, 2'-[[[(4-methoxyphenyl)acetyl]amino]methyl]-N-[2-(3-pyridinyl)ethyl]-; 2'-[[2- (4-Methoxyphenyl) acetylamino]methyl]biphenyl-2-carboxylic acid (2-pyridin-3-yl-ethyl)amide; AVE 0118; AVE0118. Grades: ≥95%. CAS No. 498577-53-0. Molecular formula: C30H29N3O3. Mole weight: 479.57. | |
| AVE 0118 hydrochloride | AVE 0118 hydrochloride is a potassium channel blocker that has the potential for the treatment of sleep apnea syndrome. AVE 0118 functions without apparent effect on ventricular repolarization. Noteworthy, the atrial selective and dose-dependent prolongation of atrial refractoriness (ERP) by AVE 0118 has been claimed to be an inhibitory effect of sodium channel activity in an atrial-selective manner, and may therefore contribute to anti-AF property of AVE0118. Synonyms: Benzeneacetamide, 4-methoxy-N-[[2'-[[[2-(3-pyridinyl)ethyl]amino]carbonyl][1,1'-biphenyl]-2-yl]methyl]-, hydrochloride (1:1); 2'-[[[2-(4-Methoxyphenyl)acetyl]amino]methyl]-N-[2-(3-pyridinyl)ethyl][1,1'-biphenyl]-2-carboxamide hydrochloride; [1,1'-Biphenyl]-2-carboxamide, 2'-[[[(4-methoxyphenyl)acetyl]amino]methyl]-N-[2-(3-pyridinyl)ethyl]-, hydrochloride; 2'-[[2- (4-Methoxyphenyl) acetylamino]methyl]biphenyl-2-carboxylic acid (2-pyridin-3-yl-ethyl)amide hydrochloride; AVE 0118 hydrochloride; AVE0118 hydrochloride. Grades: 99%. CAS No. 2108821-80-1. Molecular formula: C30H29N3O3.HCl. Mole weight: 516.03. | |
| Capsiamide | Capsiamide is a long chain amide found in essential oil of Capsicum (all hot pepper varieties). Studies showed that Capsiamide decreased spontaneous motor activity and produced a significant prolongation of sleeping time after sodium pentobarbital. Group: Biochemicals. Alternative Names: N- (13-Methyltetradecyl) acetamide; Cap-A; Capsi-amide. Grades: Highly Purified. CAS No. 64317-66-4. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Carboxylesterase 2 from Human, Recombinant | Member of a serine esterase family that hydrolyze ester and amide bonds. Carboxylesterase 2 is an endoplasmic reticulum-bound hydrolase that plays a critical role in xenobiotic detoxification and activation for ester-containing therapeutics. Carboxylesterase 2 is also involved in the detoxification of drugs such as heroin and cocaine. This enzyme is thought to play a role in lipid metabolism. Human carboxylesterase 2 (hCE-2) recognizes a substrate with a large alcohol group and small acyl group. Its substrate specificity may be restricted by a capability of acyl-hCE-2 conjugate formation due to the presence of conformational interference in the active site pocket. Carboxylesterases catalyze the biotransformation of several ester-containing drugs and prodrugs such as angiotensin-converting enzyme inhibitor (temocarpil, cilazapril), anti-tumor drugs (capecitabin) and narcotics. Group: Enzymes. Synonyms: EC 3.1.1.1; Carboxylesterase 2; CES2; CES2A1; CE-2; . Enzyme Commission Number: EC 3.1.1.1. CAS No. 9016-18-6. Purity: >95% (SDS-PAGE). Esterase. Mole weight: ~60 kDa. Activity: >30,000 (pmol/min/μg). Storage: Store at -70°C. Form: Supplied as a solution containing sodium chloride, sodium acetate, and 20% glycerol. Source: Mouse NSO cells. Species: Human. EC 3.1.1.1; Carboxylesterase 2; CES2; CES2A1; CE-2; PCE-2; iCE. Cat No: NATE-0812. |  |
| Cerebroside D | It is produced by the strain of Pachybasium sp. It has strong anti-candida albicans B311 activity in the presence of aculeacin with 0.05 ?/mL. Cerebroside D is a glycoceramide compound with antitumor activity. Study on murine experimental colitis showed that cerebroside D reduced weight loss and the macroscopic as well as microscopic appearances of colitis induced by dexran sulfate sodium. Cerebroside D also inhibited proliferation and induced apoptosis of T cells activated by concanavalin A or anti-CD3 plus anti-CD28 antibodies. Synonyms: (2S,2'R,3R,4E,8E)-N-2'-hydroxyoctadecanoyl-1-O-(β-D-glucopyranosyl)-9-methyl-4,8-sphingadienine; (R)-2-Hydroxy-octadecanoic acid [(3E,7E)-(1S,2R)-2-hydroxy-8-methyl-1-((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxymethyl)-heptadeca-3,7-dienyl]-amide. Grades: 96.5%. CAS No. 113773-89-0. Molecular formula: C43H81NO9. Mole weight: 756.117. | |
| CP-456773 sodium | CP-456773, also known as MCC950 and CRID3, is a potent, orally bioavailable NLRP3 inflammasome inhibitor and inhibits IL-1β (IC50 = 7.2 nM), IL-1α (IC50 = 12-18 nM) and IL-18 (IC50 = 10.3 nM) production for the treatment of inflammatory diseases. Synonyms: sodium ((1,2,3,5,6,7-hexahydro-s-indacen-4-yl)carbamoyl)((4-(2-hydroxypropan-2-yl)furan-2-yl)sulfonyl)amide; MCC950; MCC 950; MCC-950; CP-45677; CP45677; CP 45677; CRID-3; CRID3; CRID 3; CP-456773 sodium salt; CP 456773 sodium salt; CP456773 sodium salt; Cytokine release inhibitory drug 3. CAS No. 256373-96-3. Molecular formula: C20H24N2NaO5S. Mole weight: 427.46. | |
| Diclofenac amide | Diclofenac amide is a prodrug for Diclofenac sodium (HY-15037). Diclofenac amide is an orally active inhibitor for COX-1/2 , that inhibits the production of prostaglandins (PG) and thromboxanes (TX). Diclofenac amide exhibits anti-inflammatory efficacy in Carrageenan (HY-125474)-induced rat paw edema model without causing gastric ulcer (300 μmol/kg) [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 15362-40-0. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-134521. | |
| Diclofenac Amide | Diclofenac Amide. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: Diclofenac Sodium Imp. A (EP), Diclofenac Related Compound A (USP), Aceclofenac Imp. I (EP),1-(2,6-Dichlorophenyl)-1,3-dihydro-2H-indol-2-one. CAS No. 15362-40-0. IUPAC Name: 1-(2,6-dichlorophenyl)-3H-indol-2-one. Molecular Formula: C14H9Cl2NO. Mole Weight: 278.13. Catalog: APS15362400. SMILES: Clc1cccc(Cl)c1N2C(=O)Cc3ccccc23. Format: Neat. |  |
| glutaconyl-CoA decarboxylase | The enzyme from Acidaminococcus fermentans is a biotinyl-protein, requires Na+, and acts as a sodium pump. Prior to the Na+-dependent decarboxylation, the carboxylate is transferred to biotin in a Na+-independent manner. The conserved lysine, to which biotin forms an amide bond, is located 34 amino acids before the C-terminus, flanked on both sides by two methionine residues, which are conserved in every biotin-dependent enzyme. Group: Enzymes. Synonyms: glutaconyl coenzyme A decarboxylase; pent-2-enoyl-CoA carboxy-lyase; 4-carboxybut-2-enoyl-CoA carboxy-lyase. Enzyme Commission Number: EC 4.1.1.70. CAS No. 84399-93-9. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4818; glutaconyl-CoA decarboxylase; EC 4.1.1.70; 84399-93-9; glutaconyl coenzyme A decarboxylase; pent-2-enoyl-CoA carboxy-lyase; 4-carboxybut-2-enoyl-CoA carboxy-lyase. Cat No: EXWM-4818. | |
| Levobupivacaine free base | Levobupivacaine is a local anaesthetic drug belonging to the amino amide group. It is the S-enantiomer of bupivacaine. Levobupivacaine hydrochloride is commonly marketed by Abbott under the trade name Chirocaine. It acts via reversibly binding voltage-gated sodium channels to modulate ionic flux and block the initiation and transmission of nerve impulses. Uses: Local anaesthetic drug. Synonyms: (S)-1-butyl-N-(2,6-dimethylphenyl)piperidine-2-carboxamide; Levobupivacaine free base; (S)-1-Butyl-2',6'-pipecoloxylidide; L(-)-Bupivacaine. Grades: 98%. CAS No. 27262-47-1. Molecular formula: C18H28N2O. Mole weight: 288.44. | |
| Levobupivacaine hydrochloride | Levobupivacaine hydrochloride ((S)-(-)-Bupivacaine monohydrochloride) is a long-acting amide local agent that can suppress or relieve pain. Levobupivacaine hydrochloride exerts agent that can suppress or relieve pain. and analgesic effects through reversible blockade of neuronal sodium channel. Levobupivacaine hydrochloride can inhibit impulse transmission and conduction in cardiovascular and other tissues, possessing certain cardiac and CNS toxicity. Levobupivacaine hydrochloride is metabolized by hepatic cytochrome P450 (CYP450) enzymes in vivo. Levobupivacaine hydrochloride can also induce ferroptosis by miR-489-3p/SLC7A11 signaling in gastric cancer [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: (S)-(-)-Bupivacaine monohydrochloride. CAS No. 27262-48-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-B0653A. | |
| Lidocaine | Lidocaine (Lignocaine) inhibits sodium channels involving complex voltage and using dependence [1]. Lidocaine decreases growth, migration and invasion of gastric carcinoma cells via up-regulating miR-145 expression and further inactivation of MEK/ERK and NF-κB signaling pathways. Lidocaine is an amide derivative and has potential for the research of ventricular arrhythmia [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Lignocaine. CAS No. 137-58-6. Pack Sizes: 10 mM * 1 mL; 500 mg; 5 g; 10 g. Product ID: HY-B0185. | |
| Lidocaine-d10 | Lidocaine-d 10 is the deuterium labeled Lidocaine. Lidocaine (Lignocaine) inhibits sodium channels involving complex voltage and using dependence[1]. Lidocaine decreases growth, migration and invasion of gastric carcinoma cells via up-regulating miR-145 expression and further inactivation of MEK/ERK and NF-κB signaling pathways. Lidocaine is an amide derivative and has potential for the research of ventricular arrhythmia[2]. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 851528-09-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-B0185S1. | |
| Lidocaine-d10 hydrochloride | Lidocaine-d 10 (hydrochloride) is the deuterium labeled Lidocaine hydrochloride. Lidocaine hydrochloride (Lignocaine hydrochloride) inhibits sodium channels involving complex voltage and using dependence[1]. Lidocaine hydrochloride decreases growth, migration and invasion of gastric carcinoma cells via up-regulating miR-145 expression and further inactivation of MEK/ERK and NF-κB signaling pathways. Lidocaine hydrochloride, an amide derivative, has the potential for the research of the ventricular arrhythmia[2]. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 1189959-13-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-B0185AS. | |
| Lidocaine hydrochloride | Lidocaine hydrochloride (Lignocaine hydrochloride) inhibits sodium channels involving complex voltage and using dependence [1]. Lidocaine hydrochloride decreases growth, migration and invasion of gastric carcinoma cells via up-regulating miR-145 expression and further inactivation of MEK/ERK and NF-κB signaling pathways. Lidocaine hydrochloride is an amide derivative and a agent to treat ventricular arrhythmia and an effective tumor-inhibitor [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Lignocaine hydrochloride. CAS No. 73-78-9. Pack Sizes: 10 mM * 1 mL; 500 mg; 5 g; 10 g. Product ID: HY-B0185A. | |
| Lidocaine hydrochloride hydrate | Lidocaine (Lignocaine) hydrochloride hydrate inhibits sodium channels involving complex voltage and using dependence. Lidocaine hydrochloride hydrate decreases growth, migration and invasion of gastric carcinoma cells via up-regulating miR-145 expression and further inactivation of MEK/ERK and NF-κB signaling pathways. Lidocaine hydrochloride hydrate is an amide derivative and has potential for the research of ventricular arrhythmia [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Lignocaine hydrochloride hydrate. CAS No. 6108-05-0. Pack Sizes: 50 mg; 100 mg. Product ID: HY-B0185B. | |
| Mepivacaine | Mepivacaine is an amide-type local anesthetic agent. Mepivacaine binds to specific voltage-gated sodium ion channels in neuronal cell membranes, which inhibits both sodium influx and membrane depolarization [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 96-88-8. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-B0517. | |
| (+)-Mepivacaine | (+)-Mepivacaine is a racemic isomer of Mepivacaine (HY-B0517), which has analgesic and vasoconstrictive activity. Mepivacaine is an amide type agent that temporarily causes local loss of consciousness. Mepivacaine binds to specific voltage-gated sodium channels on neuronal cell membranes, inhibiting sodium influx and membrane depolarization [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Dexivacaine; (S)-Mepivacaine. CAS No. 24358-84-7. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-119961. | |
| NAD Synthetase from B. subtilis, Recombinant | In enzymology, a NAD+ synthase (EC 6.3.1.5) is an enzyme that catalyzes the chemical reaction:ATP + deamido-NAD+ + NH3<-> AMP + diphosphate + NAD+. The 3 substrates of this enzyme are ATP, deamido-NAD+, and NH3, whereas its 3 products are AMP, diphosphate, and NAD+. This enzyme belongs to the family of ligases, specifically those forming carbon-nitrogen bonds as acid-D-ammonia (or amine) ligases (amide synthases). This enzyme participates in nicotinate and nicotinamide metabolism and nitrogen metabolism. Group: Enzymes. Synonyms: EC 6.3.1.5; 9032-69-3; NAD+ synthetase; NAD+ synthase; nicotinamide adenine dinucleotide synthetase; diphosphopyridine nucleotide synthetase. Purity: > 98% (SDS-PAGE). NAD Synthetase. Mole weight: ~30.4kDa. Activity: ~0.3 U/mg protein. Stability: Stable for at least 6 months after receipt when stored at -80°C. Storage: Store at -20°C. After opening, prepare aliquots and store at -80°C. Avoid freeze/thaw cycles. Form: Liquid. In 50mM TRIS-HCl, pH 8, containing 75mM sodium chloride, 5% glycerol and 5mM DTT. Source: E. coli. Species: B. subtilis. EC 6.3.1.5; 9032-69-3; NAD+ synthetase; NAD+ synthase; nicotinamide adenine dinucleotide synthetase; diphosphopyridine nucleotide synthetase. Cat No: NATE-1244. | |
| Native Escherichia coli Asparaginase | Asparaginase (EC 3.5.1.1, USAN) or Colaspase (BAN) is an enzyme that catalyzes the hydrolysis of asparagine to aspartic acid. Asparaginases are enzymes expressed and produced by microorganisms. Applications: Asparaginase is used in enzymatic assays and to convert asparagine to aspartic acid. asparaginase is used to reduce the formation of acrylamide in starchy food products. it is also used as a chemotherapy agent for acute lymphoblastic leukemia. product is from escherichia coli and is provided as a lyophilized powder containing sodium chloride. Group: Enzymes. Synonyms: EC 3.5.1.1; Asparaginase; Colaspase; L-asparaginase; L-asparagine amidohydrolase. Enzyme Commission Number: EC 3.5.1.1. CAS No. 9015-68-3. Asparaginase. Storage: 2-8°C. Form: lyophilized powder. Source: Escherichia coli. EC 3.5.1.1; Asparaginase; Colaspase; L-asparaginase; L-asparagine amidohydrolase. Cat No: PHAM-226. | |
| Native Escherichia coli L-Glutamine Synthetase | Glutamine synthetase (GS) (EC 6.3.1.2) is an enzyme that plays an essential role in the metabolism of nitrogen by catalyzing the condensation of glutamate and ammonia to form glutamine:Glutamate + ATP + NH3 ? Glutamine + ADP + phosphate. Glutamine Synthetase uses ammonia produced by Nitrate reduction, amino acid degradation, and photorespiration. The amide group of glutamate is a nitrogen source for the synthesis of glutamine pathway metabolites. Applications: L-glutamine synthetase may be used for the purification of proteases from escherichia coli. Group: Enzymes. Synonyms: glutamine synthetase; glutamylhydroxamic synthetase; L-glutamine synthetase; glutamate-ammonia ligase; L-Glutamate:ammonia ligase (ADP-forming); EC 6.3.1.2; GS; 9023-70-5. Enzyme Commission Number: EC 6.3.1.2. CAS No. 9023-70-5. Purity: affinity chromatography. GS. Activity: 400-2,000 units/mg protein. Storage: -20°C. Form: lyophilized powder; Contains potassium phosphate, sodium Citrate and magnesium acetate buffer salts. Source: Escherichia coli. glutamine synthetase; glutamylhydroxamic synthetase; L-glutamine synthetase; glutamate-ammonia ligase; L-Glutamate:ammonia ligase (ADP-forming); EC 6.3.1.2; GS; 9023-70-5. Cat No: NATE-0321. | |
| Native Porcine Elastase | Pancreatic elastase is a form of elastase that is produced in the acinar cells of the pancreas, initially produced as an inactive zymogen and later activated in the duodenum by trypsin. Elastases form a subfamily of serine proteases, characterized by a distinctive structure consisting of two beta barrel domains converging at the active site that hydrolyze amides and esters amongst many proteins in addition to elastin, a type of connective tissue that holds organs together. Pancreatic elastase 1 is a serine endopeptidase, a specific type of protease that has the amino acid serine at its active site. Group: Enzymes. Synonyms: EC 3.4.21.36, pancreatopeptidase E; pancreatic elastase I; elastase; elaszym; serine elastase; elastase-1; pancreatopeptidase; ELA1. Enzyme Commission Number: EC 3.4.21.36. CAS No. 39445-21-1. ELA1. Activity: Type I, > 15 units/mg; Type II, > 4.0 units/mg protein; Type III, > 1 units/mg protein (biuret). Storage: -20°C. Form: Type I, white powder; Type II, Type III, lyophilized powder, Contains sodium carbonate. Source: Porcine pancreas. Species: Porcine. EC 3.4.21.36, pancreatopeptidase E; pancreatic elastase I; elastase; elaszym; serine elastase; elastase-1; pancreatopeptidase; ELA1. Pack: Package size based on protein content. Cat No: NATE-0211. | |
| Parecoxib Sodium | Parecoxib Sodium. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Sodium (4-(5-methyl-3-phenylisoxazol-4-yl)phenylsulfonyl)(propionyl)amide. CAS No. 198470-85-8. Molecular formula: C19H17N2NaO4S. Mole weight: 392.4. Purity: ≥98%. Product ID: ACM198470858. Alfa Chemistry ISO 9001:2015 Certified. | |
| Ropivacaine mesylate | Ropivacaine mesylate is a long-acting amide local anaesthetic agent for a spinal block and effectively blocks neuropathic pain. Ropivacaine blocks impulse conduction via reversible inhibition of sodium ion influx in nerve fibressup>[1] [2]. Ropivacaine is also an inhibitor of K 2P (two-pore domain potassium channel) TREK-1 with an IC 50 of 402.7 μM in COS-7 cell's membrane [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 854056-07-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-B0563C. | |
| Rosuvastatin Impurity 34 | Rosuvastatin Impurity 34. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: sodium (5-((3S,5R,E)-6-carboxylato-3,5-dihydroxyhex-1-en-1-yl)-4-(4-fluorophenyl)-6-isopropylpyrimidin-2-yl)(methylsulfonyl)amide. CAS No. 371775-74-5. Molecular Formula: C21H24FN3Na2O6S. Mole Weight: 511.47. Catalog: APB371775745. | |
| Sodium glycocholate hydrate | Sodium glycocholate hydrate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 3α,7α,12α-Trihydroxy-5β-cholan-24-oic acid N-(carboxymethyl)amide sodium salt. CAS No. 338950-81-5. Molecular formula: C26H42NO6Na·xH2O. Mole weight: 487.60 (anhydrous basis). Purity: ≥95%. IUPACName: sodium;2-[4-(3,7,12-trihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoylamino]acetate;hydrate. Canonical SMILES: CC(CCC(=O)NCC(=O)[O-])C1CCC2C1(C(CC3C2C(CC4C3(CCC(C4)O)C)O)O)C.O.[Na+]. ECNumber: 212-730-9. Product ID: ACM338950815. Alfa Chemistry ISO 9001:2015 Certified. | |
| Stearic acid 2-((2-aminoethyl)amino)ethanol 2-carboxyethylated sodium salts complex | Stearic acid 2-((2-aminoethyl)amino)ethanol 2-carboxyethylated sodium salts complex. Uses: Designed for use in research and industrial production. Additional or Alternative Names: EINECS 272-378-7, EINECS 274-766-1, EINECS 274-838-2, CID162225, Octadecanoic acid, reaction products with 2-((2-aminoethyl)amino)ethanol, 68815-50-9, 70693-42-4, 70750-11-7, Octadecanoic acid, reaction products with 2-((2-aminoethyl)amino)ethanol, 2-carboxyethylated 2-hydroxyethylated, Octadecanoic acid, reaction products with 2-((2-aminoethyl)amino)ethanol, 2-carboxyethylated, sodium salts, Stearic acid, aminoethylethanolamine amide-imidazoline, methyl acrylate alkylated, saponified, sodium salt, Stearic acid, aminoethylethanolamine reaction product, alkylated with chloroacetic acid and ethylenechlorohydrin. Product Category: Heterocyclic Organic Compound. CAS No. 70693-42-4. Molecular formula: C22H48N2O3. Mole weight: 388.628120 [g/mol]. Purity: 0.96. IUPACName: 2-(2-aminoethylamino)ethanol; octadecanoic acid. Product ID: ACM70693424. Alfa Chemistry ISO 9001:2015 Certified. | |
| Sulfaclozine Sodium Monohydrate | Sulfaclozine is a competitive antagonist of para-aminobenzoic acid (PABA), a precursor of folic acid, in protozoa and bacteria. It is indicated for treatment of coccidiosis in poultry due to infection with Eimeria species, fowl typhoid due to infection with Salmonella gallinarum and fowl cholera due to infection with Pasteurella multocida. Group: Biochemicals. Alternative Names: Sodium sulfachloropyrazine monohydrate; sodium ( (4-aminophenyl)sulfonyl) (6-chloropyrazin-2-yl)amide hydrate. Grades: Highly Purified. CAS No. 1392129-96-2. Pack Sizes: 50mg. Molecular Formula: C10H8ClN4O2SNa·H2O, Molecular Weight: 324.72. US Biological Life Sciences. | Worldwide |
| Sulfuric acid isopropyl sodium salt | Sulfuric acid isopropyl sodium salt, a vital chemical component, functions as an organic synthesis catalyst. Its unparalleled proficiency in the creation of ester bonds solidifies its ubiquity in amide and nitro compound syntheses, among other organic substances. Furthermore, this chemical compound displays promising capabilities as a treatment for specific types of cancer, as well as drug-resistant tuberculosis, promoting its significance in therapeutic advancements. Synonyms: Sodiumisopropylsulfate. CAS No. 52096-25-0. Molecular formula: C3H7NaO4S. Mole weight: 162.14. | |
| Tauro-α-muricholic acid sodium salt | Tauro-α-muricholic acid is an antagonist of the farnesoid X receptor (FXR) with IC50 value of 28 μM. Synonyms: 5β-cholanic acid-3α,6β,7α-triol N-(2-sulphoethyl)-amide, sodium salt; Taro-α-muricholate; TαMCA; 2-[[(3α, 5β, 6β, 7α)-3, 6, 7-trihydroxy-24-oxocholan-24-yl]amino]-ethanesulfonic acid, monosodium salt. Grades: ≥95%. CAS No. 2260905-08-4. Molecular formula: C26H44NNaO7S. Mole weight: 537.69. | |
| Tauro-β-muricholic acid sodium salt | Tauro-β-muricholic acid is a competitive and reversible antagonist of the farnesoid X receptor (FXR) with IC50 value of 40 μM. Synonyms: 5beta-cholanic acid-3alpha,6beta,7beta-triol N-(2-sulphoethyl)-amide, sodium salt; 2-[[(3alpha,5beta,6beta,7beta)-3,6,7-trihydroxy-24-oxocholan-24-yl]amino]-ethanesulfonic acid, monosodium salt. Grades: ≥95%. CAS No. 145022-92-0. Molecular formula: C26H44NNaO7S. Mole weight: 537.69. | |
| tBuBrettPhos Pd G3 | tBuBrettPhos Pd G3. Uses: Palladium catalyst used for the arylation of primary amides. palladium catalyst used for the synthesis of n-aryl carbamates. palladium catalyst used for the n-monoarylation of amidines. palladium catalyst used for the cross-coupling of aryl chlorides and triflates with sodium cyanate - a practical synthesis of unsymmetrical ureas. palladium catalyst used in the synthesis of imidazo[4,5-b]pyridines and imidazo[4,5]pyrazines through amidation of 2-chloro-3-amino-heterocycles. palladium catalyst used in the n-arylation of 2-aminothiazoles palladium catalyst used in the synthesis of diarylethers under mild conditions. palladium catalyst used in the hydroxylation of aryl and heteroaryl halides. Additional or Alternative Names: Ditert-butyl-[3,6-dimethoxy-2-[2,4,6-tri(propan-2-yl)phenyl]phenyl]phosphane;methanesulfonic acid;palladium;2-phenylaniline. Appearance: Solid. CAS No. 1536473-72-9. Molecular formula: C44H63NO5PPdS. Mole weight: 855.4. Purity: 0.98. Canonical SMILES: CC(C)C1=CC(=C(C(=C1)C(C)C)C2=C(C=CC(=C2P(C(C)(C)C)C(C)(C)C)OC)OC)C(C)C.CS(=O)(=O)O.C1=CC=C([C-]=C1)C2=CC=CC=C2N.[Pd]. Product ID: ACM1536473729-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| 2- {N2- [Na-Benzoyl benzoicamido-N6-6-biotinamidocaproyl ] lysinyl amido} ethyl -2- (N-sulfosuccinimidyl carboxy) ethyl Disulfide, Sodium Salt | An amine reactive trifunctional cross linker. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| 2-Pyrimidinecarboximidam ide Hydrochloride | Contains up to 5 % Sodium Acetate by weight. Group: Biochemicals. Alternative Names: 2-Amidinopyrimidine Hydrochloride; 2-Pyrimidinecarboximidam ide Monohydrochloride. Grades: Highly Purified. CAS No. 138588-40-6. Pack Sizes: 500mg, 5g, 10g. US Biological Life Sciences. | Worldwide |
| 5-Bromo-CTP | 5-Bromo-CTP is a nucleotide analog renowned in the field of compound, emerging as an indispensible asset for scrutinizing RNA research and development and transcription. Its utility lies particularly in metabolic labeling experiments, enabling profound exploration into RNA and mRNA modifications as well as unraveling the intricate dynamics of RNA sequence evolution amidst mutations. Synonyms: (5Br-CTP); 5-Bromo-cytidine-5'-triphosphate, Sodium salt. Grades: ≥ 95% by HPLC. Molecular formula: C9H15N3O14P3Br (free acid). Mole weight: 562.05 (free acid). | |
| 5-Propargylamino-ddUTP | 5-Propargylamino-ddUTP is an innovative biomedical substance, acting as a modified nucleotide. It efficaciously integrates into DNA amidst replication, ingeniously orchestrating the halt of DNA research and development. The versatile nature of this compound allows for its multifaceted employment in diverse domains, ranging from precise identification and tracing of distinctive DNA sequences to profound explorations into the intricate nexus of DNA-protein interactions. Synonyms: 5-Propargylamino-2',3'-dideoxyuridine-5'-triphosphate, Sodium salt. Grades: ≥ 95% by HPLC. Molecular formula: C12H18N3O13P3 (free acid). Mole weight: 505.20 (free acid). | |
| Acid Black 2 | Acid Black 2 is a synthetic dye belonging to the triphenylmethane family. Acid Black 2 is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Acid black 2 is widely used in a variety of scientific research applications. it is used in the study of cell structure and function, as well as in the study of enzymes and proteins. it is also used in the study of gene expression and in the study of metabolic pathways. nigrosine can also be used in the study of plant and animal physiology, as well as in the study of biochemistry. Additional or Alternative Names: Black 10B; Vondamol Light Black 10B; Dinatrium-4-amino-5-hydroxy-3-[(E)-(4-nitrophenyl)diazenyl]-6-[(E)-phenyldiazenyl]-2,7-naphthalendisulfonat; Fast Sulon Black BN; Metamine Blue Black; Amido Black 10 B; Naphtocard Black 12B ; Aniline blue black; CI NO 0470; Sodium 4-amino-5-hydroxy-3-(4-nitrophenylazo)-6-(phenylazo)naphthalene-2,7-disulphonate; Comacid Blue Black B; Calcocid Blue Black 2R. Product Category: Acid Dyes. Appearance: dark brown granular solid. CAS No. 8005-3-6. Molecular formula: C22H14N6Na2O9S2. Mole weight: 616.491. IUPACName: disodium;4-amino-5-hydroxy-3-[(4-nitrophenyl)diazenyl]-6-phenyldiazenylnaphthalene-2,7-disulfonate. Canonical SMILES: C1=CC=C(C=C1)N=NC2=C(C3=C(C(=C(C=C3C=C2S(=O)(=O)[O-])S(=O)(=O)[O-])N=NC4=CC=C(C=C4)[N+](=O)[O-])N)O.[Na+].[Na+]. Product ID: ACM8005036. Alfa Chemi | |
| Acid Red 1 | Acid Red 1. Group: Biochemicals. Alternative Names: 1379 Red; Acetyl Red G; Acetyl Red J; Acetyl Rose 2GL; Acid Bright Red; Acid Brilliant Fuchsine 2G; Acid Brilliant Red; Acid Fast Red 3G; Acid Fast Red EG; Acid Fast Red EGG; Acid Geranine 2G; Acid Geranine 2GN; Acid Leather Red KG; Acid Naftol Red G; Acid Naphthol Red G; Acid Phloxine GA; Acid Red 1; Acid Red 2G; Acid Red G; Acid Red GA; Acid Red GN; Acid Red Geramine G; Acid Rose 2GL; Acidal Brilliant Red 2G; Acidine Red G; Acilan Naphthol Red G; Ahcocid Carmine 2G; Amacid Phloxine G; Amacid Phloxine G Conc; Amecid Floxine 2GN; Amido Naphthol Red 2G; Amido Naphthol Red G; Amido Naphthol Red GA; Amido Red 2G; Atul Acid Geranine G; Azo...iton Red G; Leather Red G; Lignin Pink; Lissamine Red 2G; Monacid Red 2G; Multacid Red G; Multicuer Red G; Naphthazine Rose 2G; Naphtocard Red 2G; Neolan Red E 2GN; Phloxine 2G; Phloxine G; Pontacyl Carmine 2G; Ravi Acid Red AG; Red 2G; Ritacid Red S; Sandolan Rhodine E 2GL; Sandolan Rhodine E 2GLI; Solar Fast Red 3G; Triacid Amidonaphthol Red G; Triacid Light Red G; Unitertracid Red 2G; Vibra Color Red ARE 1; Vondacid Light Red NG; Water Red 177614; 5-(Acetylamino)-4-hydroxy-3-(2-phenyldiazenyl)-2,7-naphthalenedisulfonic Acid Sodium Salt. Grades: Highly Purified. CAS No. 3734-67-6. Pack Sizes: 5g. Molecular Formula: C18H13N3NaO8S2, Molecular Weight: 509.42. US Biological Life Sciences. | Worldwide |
| Acid Red 52 | Dyes & Metabolites; Dyes & Metabolites. Uses: For analytical and research use. Group: Reagents. Alternative Names: Orient Water Red 27, Brilliant Superlan Rhodamine B, Colocid Rhodamine BH, Aizen Food Red No. 106, Daiwa Red 106WB, Kayacyl Rhodamine FB, Indacid Rhodamine B, Sandolan Rhodamine E-B 400, Amido Rhodamine B, Acid Rose B, Duasyn Acid Rhodamine B 01, Nylosan Rhodamine B, Kiton Red 620, Triacid Rhodamine B, Rhodamine Acid, [6-(Diethylamino)-9-(2,4-disulfophenyl)-3H-xanthen-3-ylidene]diethylammonium hydroxide inner salt sodium salt, Acid Red XB, Food Red No. 106, Colocid Rhodamine BN, Lissamine Rhodamine B 200, Conacid Red EB, Red 106, Hispacid Brilliant Pink B, Pacid Rhodamine ...ed 106, Lissamine Rhodamine B, Rhodamine 200S, Pro-Jet Red OAM, Rhodamine B, Kemacid Rhodamine B, Red no. 106, Brilliant Superlan Rhodamine 2B, Japan Red No. 106, Sulforhodamin B, C.I. 45100, Solar Rhodamine B, Kayaku Acid Rhodamine FB, Kiton Rhodamine B, Sulforhodamine B, 3,6-bis(Diethylamino)-9-(2,4-disulfophenyl)xanthylium inner salt sodium salt, Acid Red 52, Fenazo Pink XXB, Japan Red 106, Kiton Red S, Dyacid Red 4B, Ravi Acid Rhodamine B,3,6-Bis(diethylamino)-9-(2,4-disulfophenyl)xanthylium inner salt sodium salt (1:1), C.I. Acid Red 52, Duramine Rhodamine B, Acid Rhodamine, Phloxine rhodamine, Sandolan Rhodamine E-B. CAS No. 3520-42-1. IUPAC Name: sodium;4-[3,6-bis(diethylamino)xa | |
| AppNH2 | AppNH2 is indispensable in research of combating ailments including cancer, diabetes is and autoimmune disorders. This revolutionary creation assuming the role of both a mighty inhibitor and a formidable activator, skillfully honing in on crucial proteins and enzymes entangled in the labyrinthine pathways of pathological advancement. Profoundly effective is appNH2 harnesses its exceptional chemical attributes to govern intricate cellular dynamics, thereby fostering optimal physiological harmony. Synonyms: (AMPPN); Adenosine-5'-(β-amido)diphosphate, Sodium salt. Grades: ≥ 95% by HPLC. Molecular formula: C10H16N6O9P2 (free acid). Mole weight: 426.21 (free acid). | |
| Bentiromide | Bentiromide. Uses: Designed for use in research and industrial production. Additional or Alternative Names: bentiromide, 13135_FLUKA, 13135_SIGMA, MolPort-003-926-261, EINECS 255-530-7, N-Benzoyl-L-tyrosine p-amidobenzoic acid sodium salt, N-Benzoyl-L-tyrosyl-4-aminobenzoic acid sodium salt, Sodium (S)-4-((2-(benzoylamino)-3-(4-hydroxyphenyl)-1-oxopropyl)amino)benzoate, 41748-47-4. Product Category: Heterocyclic Organic Compound. Appearance: powder. CAS No. 41748-47-4. Molecular formula: C23H19N2NaO5. Mole weight: 426.4. Purity: 0.96. IUPACName: sodium 4-[[(2S)-2-benzamido-3-(4-hydroxyphenyl)propanoyl]amino]benzoate. Canonical SMILES: C1=CC=C(C=C1)C(=O)NC(CC2=CC=C(C=C2)O)C(=O)NC3=CC=C(C=C3)C(=O)[O-].[Na+]. ECNumber: 253-349-8. Product ID: ACM41748474. Alfa Chemistry ISO 9001:2015 Certified. | |
| β-Lactamase Blend, Recombinant | β--lactamase inactivates β-lactam antibiotics by breaking open the β-lactam ring. Group: Enzymes. Synonyms: β-lactamase; penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase; EC 3.5.2.6; 9073-60-3. Enzyme Commission Number: EC 3.5.2.6. CAS No. 9073-60-3. β-Lactamase. Activity: 600-1500 IU beta-lactamase I per vial; 60-100 IU beta-lactamase II per vial. Storage: 2-8°C. Form: Lyophilized powder containing sodium chloride, potassium phosphate and sorbitol. Source: E. coli. β-lactamase; penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase; EC 3.5.2.6; 9073-60-3. Cat No: NATE-0776. | |
| β-Lactamase from Pseudomonas aeruginosa, Recombinant | β--lactamase inactivates β-lactam antibiotics by breaking open the β-lactam ring. Applications: Β-lactamase is used to inactivate β-lactam antibiotics by breaking open the β-lactam ring. β-lactamase is used to study antibiotic resistance and resistance suppression. product is produced from pseudomonas aeruginosa and is expressed in e. coli. Group: Enzymes. Synonyms: β-lactamase; penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase; EC 3.5.2.6; 907. Enzyme Commission Number: EC 3.5.2.6. CAS No. 9073-60-3. β-Lactamase. Activity: > 20 U/mg (with cephalosporin C); > 400 U/mg (with benzylpenicilin). Storage: 2-8°C. Form: Lyophilized powder containing sodium chloride and potassium phosphate. Source: E. coli. Species: Pseudomonas aeruginosa. β-lactamase; penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase; EC 3.5.2.6; 9073-60-3. Cat No: NATE-0777. | |
| (+)-Biotin 4-amidobenzoic acid sodium salt | (+)-Biotin 4-amidobenzoic acid sodium salt is a crucial compound used in the biomedical industry. It acts as a precursor for designing novel drugs targeting biotin-dependent enzymes, aiding in the treatment of various disorders related to biotin deficiencies. Synonyms: 4-[[5-[(3aS,4S,6aR)-Hexahydro-2-oxo-1H-thieno[3,4-d]imidazol-4-yl]-1-oxopentyl]amino]benzoic acid sodium salt; N-Biotinyl-p-aminobenzoic acid sodium salt. CAS No. 102418-74-6. Molecular formula: C17H20N3NaO4S. Mole weight: 385.41. | |
| (+)-Biotin 4-Amidobenzoic Acid, Sodium Salt (N-Biotinyl-p-aminobenzoic Acid) | A fluorigenic substrate for the determination of Biotinidase activity. Group: Biochemicals. Alternative Names: (+)-Biotin 4-Amidobenzoic Acid, Sodium Salt; 4- [ [5- [ (3aS, 4S, 6aR) -Hexahydro-2-oxo-1H-thieno [3, 4-d] imidazol-4-yl] -1-oxopentyl] amino] benzoic Acid Sodium Salt; N-Biotinyl-p-aminobenzoic Acid Sodium Salt. Grades: Highly Purified. CAS No. 102418-74-6. Pack Sizes: 100mg, 250mg, 500mg. Molecular Formula: C17H20N3NaO4S, Molecular Weight: 385.41. US Biological Life Sciences. | Worldwide |
| Diatrizoic acid sodium salt dihydrate | Diatrizoic acid sodium salt dihydrate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Diatrizoate sodium, Histopaque, Iothalamate, Triombrine, Triombrin, Vascoray, Hypaque, Methalamic acid, Hypaque sodium, Sodium diatrizoate, Hypaque Cysto, Gastrografin, Hypaque-DIU, Urovist sodium, Sodium amidotrizoate, Hypaque 50, Meglumine diatrizoate, Conray 35, Urovist Sodium 300, Diatrizoate sodium salt. Product Category: Heterocyclic Organic Compound. CAS No. 737-31-5. Molecular formula: C11H8I3N2NaO4. Mole weight: 635.9. Purity: Purity >98%. IUPACName: sodium 3,5-diacetamido-2,4,6-triiodobenzoate. Canonical SMILES: CC(=O)NC1=C(C(=C(C(=C1I)C(=O)[O-])I)NC(=O)C)I.[Na+]. ECNumber: 212-004-1. Product ID: ACM737315. Alfa Chemistry ISO 9001:2015 Certified. | |
| GM1-Lysoganglioside sodium | GM1-Lysoganglioside sodium, a highly esteemed biomedical agent, stands as a fostering solution amidst the intricate realm of neurodegenerative afflictions like Parkinson's disease and Alzheimer's disease. Synonyms: lyso-Monosialoganglioside GM1; Lyso-GM1. Grades: 95%. CAS No. 94458-59-0. Molecular formula: C55H97N3O30·xNa. Mole weight: 1280.36 (free acid). | |
| N-acetylglucosamine 6-phosphate deacetylase from Bacillus subtilis, Recombinant | In enzymology, a N-acetylglucosamine-6-phosphate deacetylase (EC 3.5.1.25) is an enzyme that catalyzes the chemical reaction: N-acetyl-D-glucosamine 6-phosphate + H2O ? D-glucosamine 6-phosphate + acetate. Thus, the two substrates of this enzyme are N-acetyl-D-glucosamine 6-phosphate and H2O, whereas its two products are D-glucosamine 6-phosphate and acetate. Group: Enzymes. Synonyms: N-acetyl-D-glucosamine-6-phosphate amidohydrolase; acetylglucosamine phosphate deacetylase; acetylaminodeoxyglucosephosphate acetylhydrolase; 2-acetamido-2-deoxy-D-glucose-6-phosphate amidohydrolase; EC 3.5.1.25. Enzyme Commission Number: EC 3.5.1.25. CAS No. 9027-50-3. Purity: >90% as judged by SDS-PAGE. N-acetylglucosamine 6-phosphate deacetylase. Mole weight: 44.6 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacillus subtilis. N-acetyl-D-glucosamine-6-phosphate amidohydrolase; acetylglucosamine phosphate deacetylase; acetylaminodeoxyglucosephosphate acetylhydrolase; 2-acetamido-2-deoxy-D-glucose-6-phosphate amidohydrolase; EC 3.5.1.25. Cat No: NATE-1541. | |
| N-acetylglucosamine 6-phosphate deacetylase from Escherichia coli, Recombinant | In enzymology, a N-acetylglucosamine-6-phosphate deacetylase (EC 3.5.1.25) is an enzyme that catalyzes the chemical reaction: N-acetyl-D-glucosamine 6-phosphate + H2O ? D-glucosamine 6-phosphate + acetate. Thus, the two substrates of this enzyme are N-acetyl-D-glucosamine 6-phosphate and H2O, whereas its two products are D-glucosamine 6-phosphate and acetate. Group: Enzymes. Synonyms: N-acetyl-D-glucosamine-6-phosphate amidohydrolase; acetylglucosamine phosphate deacetylase; acetylaminodeoxyglucosephosphate acetylhydrolase; 2-acetamido-2-deoxy-D-glucose-6-phosphate amidohydrolase; EC 3.5.1.25. Enzyme Commission Number: EC 3.5.1.25. CAS No. 9027-50-3. Purity: >90% as judged by SDS-PAGE. N-acetylglucosamine 6-phosphate deacetylase. Mole weight: 43.0 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Escherichia coli. N-acetyl-D-glucosamine-6-phosphate amidohydrolase; acetylglucosamine phosphate deacetylase; acetylaminodeoxyglucosephosphate acetylhydrolase; 2-acetamido-2-deoxy-D-glucose-6-phosphate amidohydrolase; EC 3.5.1.25. Cat No: NATE-1540. | |
| Native Enterobacter cloacae β-Lactamase | β--lactamase inactivates β-lactam antibiotics by breaking open the β-lactam ring. Protein determined by biuret. Applications: Β-lactamase is used to inactivate β-lactam antibiotics by breaking open the β-lactam ring. β-lactamase is used to study antibiotic resistance and resistance suppression1. this product is produced from enterobacter cloacae. Group: Enzymes. Synonyms: β-lactamase; penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase; EC . Enzyme Commission Number: EC 3.5.2.6. CAS No. 9073-60-3. β-Lactamase. Activity: 6-18 units/mg protein (using benzylpenicillin); 0.2-0.6 units/mg protein (using benzylpenicillin). Storage: 2-8°C. Form: Lyophilized powder containing sodium phosphate and sodium Citrate buffer salts. Source: Enterobacter cloacae. β-lactamase; penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase; EC 3.5.2.6; 9073-60-3. Cat No: NATE-0774. | |
| Native Pseudomonas fluorescens β-Lactamase | β--lactamase inactivates β-lactam antibiotics by breaking open the β-lactam ring. Group: Enzymes. Synonyms: β-lactamase; penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase; EC 3.5.2.6; 9073-60-3. Enzyme Commission Number: EC 3.5.2.6. CAS No. 9073-60-3. β-Lactamase. Storage: 2-8°C. Form: Lyophilized powder containing potassium phosphate and sodium bicarbonate. Source: Pseudomonas fluorescens. β-lactamase; penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase; EC 3.5.2.6; 9073-60-3. Cat No: NATE-0775. | |
| Peptidoglycan N-acetylglucosamine deacetylase from Streptococcus pneumoniae, Recombinant | Peptidoglycan-N-acetylglucosamine deacetylase (EC 3.5.1.104, HP310, PgdA, SpPgdA, BC1960, peptidoglycan deacetylase, N-acetylglucosamine deacetylase, peptidoglycan GlcNAc deacetylase, peptidoglycan N-acetylglucosamine deacetylase, PG N-deacetylase) is an enzyme with systematic name peptidoglycan-N-acetylglucosamine amidohydrolase. This enzyme catalyses the following chemical reaction: peptidoglycan-N-acetyl-D-glucosamine + H2O ? peptidoglycan-D-glucosamine + acetate. This enzyme contributes to virulence of Helicobacter pylori, Listeria monocytogenes and Streptococcus suis. Group: Enzymes. Synonyms: Peptidoglycan-N-acetylglucosamine de. Enzyme Commission Number: EC 3.5.1.-. Purity: >90% as judged by SDS-PAGE. Peptidoglycan N-acetylglucosamine deacetylase. Mole weight: 24.2 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Streptococcus pneumoniae. Peptidoglycan-N-acetylglucosamine deacetylase; EC 3.5.1.-; HP310; PgdA; SpPgdA; BC1960; peptidoglycan deacetylase; N-acetylglucosamine deacetylase; peptidoglycan GlcNAc deacetylase; peptidoglycan N-acetylglucosamine deacetylase; PG N-deacetylase. Cat No: NATE-1539. | |
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